Nitric oxide-sensing actuators for modulating structure in lipid-based liquid crystalline drug delivery systems

2017 ◽  
Vol 508 ◽  
pp. 517-524 ◽  
Author(s):  
Qingtao Liu ◽  
Jinming Hu ◽  
Michael R. Whittaker ◽  
Thomas P. Davis ◽  
Ben J. Boyd
2019 ◽  
Vol 24 (7) ◽  
pp. 1405-1412 ◽  
Author(s):  
Thiagarajan Madheswaran ◽  
Murugesh Kandasamy ◽  
Rajendran JC Bose ◽  
Vengadeshprabhu Karuppagounder

2009 ◽  
Vol 18 (5) ◽  
pp. 404-411 ◽  
Author(s):  
Rita Muzzalupo ◽  
Lorena Tavano ◽  
Fiore Pasquale Nicoletta ◽  
Sonia Trombino ◽  
Roberta Cassano ◽  
...  

2019 ◽  
Vol 4 (3) ◽  
pp. 160-175 ◽  
Author(s):  
Salome A. Chime ◽  
Paul A. Akpa ◽  
Anthony A. Attama

Lipid based excipients have gained popularity recently in the formulation of drugs in order to improve their pharmacokinetic profiles. For drugs belonging to the Biopharmaceutics Classification System (BCS) class II and IV, lipid excipients play vital roles in improving their pharmacokinetics properties. Various nanocarriers viz: Solid lipid nanoparticles, nanostructured lipid carriers, selfnanoemulsifying drug delivery systems (SNEDDS), nanoliposomes and liquid crystal nanoparticles have been employed as delivery systems for such drugs with evident successes. Lipid-based nanotechnology have been used to control the release of drugs and have utility for drug targeting and hence, have been used for the delivery of various anticancer drugs and for colon targeting. Drugs encapsulated in lipids have enhanced stability due to the protection they enjoy in the lipid core of these nanoformulations. However, lipid excipients could be influenced by factors which could affect the physicochemical properties of lipid-based drug delivery systems (LBDDS). These factors include the liquid crystalline phase transition, lipid crystallization and polymorphism amongst others. However, some of the physicochemical properties of lipids made them useful as nanocarriers in the formulation of various nanoformulations. Lipids form vesicles of bilayer which have been used to deliver drugs and are often referred to as liposomes and nanoliposomes. This work aims at reviewing the different classes of lipid excipients used in formulating LBDDS and nanoformulations. Also, some factors that influence the properties of lipids, different polymorphic forms in lipid excipients that made them effective nanocarriers in nano-drug delivery would be discussed. Special considerations in selecting lipid excipients used in formulating various forms of nanoformulations would be discussed.


Author(s):  
Jayvadan Patel ◽  
Anand Shah

Self-emulsifying drug delivery systems (SEDDS) are a type of emulsion that have received particular attention in recent years as a means of enhancing oral bioavailability of poorly absorbed drugs. These systems are ideally isotropic mixture of oil and surfactant (sometimes co-surfactant are added) that form emulsions on mixing with water with little or no energy input. Hydrophobic drugs are dissolved in SEDDS. After administering the drug by this system, emulsion is formed in the GIT by selfemulsification. Generally by this process bioavailability of the drug is increased and quantity required to exert desired effect is decreased. Oil surfactant ratio, amount of surfactant, type of surfactant, nature of oil affect the process of emulsification. In the emulsification process water penetrates into the oil water interface, leading to the formation of liquid crystalline phase, resulting in swelling at the interface. Generally, SEDDS are formed with triglyceride oils and nonionic surfactant. In the GIT, during the digestion of fat, drugs are getting released and lead to increase the absorption of drug by dissolution or by particle charges which increase the bioavailability. Some latest related to SEDDS is described in this review.


2016 ◽  
Vol 2016 ◽  
pp. 1-9
Author(s):  
Lu Xiao ◽  
Tao Yi ◽  
Ying Liu ◽  
Hua Zhou

The purpose of this study was to offer a new insight into the microstructure changes duringin vitrolipolysis of five lipid-based drug delivery formulations belonging to different lipid formulation types. Five lipid-based formulations of indomethacin were investigated using anin vitrolipolysis model. During lipolysis, microstructures of the intermediate phase formed by lipolytic products were observed. The results showed that the time of liquid crystal formation duringin vitrodigestion for these formulations was Type I > Type II > Type IIIB > Type IV > Type IIIA (p<0.05). After lipolysis, the drug releases from these formulations were determined. The results showed that the amount of drug distributed in the aqueous phase, obtained by ultracentrifuge after lipolysis, was, astonishingly, in inverse rank order of the above mentioned, that is, Type IIIA > Type IV > Type IIIB > Type II > Type I (p<0.05). These results showed that the liquid crystalline phase probably has a critical influence on the fate of the drug duringin vitrolipolysis and suggested that the liquid crystalline phase facilitated drug precipitation. These findings may improve the understanding of lipolysis of lipid-based drug delivery systems for designing better delivery system.


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